A peptide derived from TID1S rescues frataxin deficiency and mitochondrial defects in FRDA cellular models
Friedreich's ataxia (FRDA), the most common recessive inherited ataxia, results from homozygous guanine-adenine-adenine (GAA) repeat expansions in intron 1 of the FXN gene, which leads to the deficiency of frataxin, a mitochondrial protein essential for iron-sulphur cluster synthesis. The study...
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Frontiers Media S.A.,
2024-03-01T00:00:00Z.
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A1234.567 |
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